84522-502 NDC - ITAMIN C POTENT NOURISH SKIN WHITE ()

Drug Information

  • Product NDC: 84522-502
  • Proprietary Name: Itamin C Potent Nourish Skin White
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Yiwu Xinqian E Commerce Co Ltd
Product Type:
FDA Application Number: M016
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:12/13/2024

Package Information

No. Package Code Package Description Billing Unit
184522-502-015 g in 1 BOX (84522-502-01)
284522-502-0215 g in 1 BOX (84522-502-02)
384522-502-0330 g in 1 BOX (84522-502-03)
484522-502-0450 g in 1 BOX (84522-502-04)
584522-502-05100 g in 1 BOX (84522-502-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC84522-502The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEItamin C Potent Nourish Skin WhiteThe labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
START MARKETING DATE12/13/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThis is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
APPLICATION NUMBERM016This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEYiwu Xinqian E Commerce Co LtdName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/19/2025

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